Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Type Device Class Implantable

Show Filters

HI-LINE XS DISP.ROSEN BURR I+ D1.0MM
Aesculap AG
GE471SU
In Commercial Distribution

  • 04046963816261 ()
GE471SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR I D0.6MM
Aesculap AG
GE469SU
In Commercial Distribution

  • 04046963816247 ()
GE469SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I+ D2.7MM
Aesculap AG
GE465SU
Not in Commercial Distribution

  • 04046963816230 ()
GE465SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I D0.8MM
Aesculap AG
GE460SU
In Commercial Distribution

  • 04046963816223 ()
GE460SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I D0.6MM
Aesculap AG
GE459SU
In Commercial Distribution

  • 04046963816216 ()
GE459SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR X-CRS.I D5.0MM
Aesculap AG
GE457SU
In Commercial Distribution

  • 04046963816209 ()
GE457SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR X-CRS.I D4.0MM
Aesculap AG
GE456SU
In Commercial Distribution

  • 04046963816193 ()
GE456SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.DIAMOND BURR II D4.0MM
Aesculap AG
GE817SU
In Commercial Distribution

  • 04046963935214 ()
GE817SU

  • Orthopaedic bur, single-use
HI-LINE XXS DIAM.NEURO CUTTER II D5.0MM
Aesculap AG
GE815SU
Not in Commercial Distribution

  • 04046963935207 ()
GE815SU

  • Orthopaedic bur, single-use
HI-LINE XXS DIAM.NEURO CUTTER II D4.0MM
Aesculap AG
GE814SU
In Commercial Distribution

  • 04046963935191 ()
GE814SU

  • Orthopaedic bur, single-use
< 1 ... 42 43 44 45 46 ... 122 >